[Congressional Bills 118th Congress]
[From the U.S. Government Publishing Office]
[S. 36 Introduced in Senate (IS)]
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118th CONGRESS
1st Session
S. 36
To review domestic biopharmaceutical manufacturing capabilities in
order to improve public health and medical preparedness and response
capabilities and domestic biopharmaceutical manufacturing capabilities.
_______________________________________________________________________
IN THE SENATE OF THE UNITED STATES
January 24 (legislative day, January 3), 2023
Mr. Rubio (for himself and Mr. Coons) introduced the following bill;
which was read twice and referred to the Committee on Health,
Education, Labor, and Pensions
_______________________________________________________________________
A BILL
To review domestic biopharmaceutical manufacturing capabilities in
order to improve public health and medical preparedness and response
capabilities and domestic biopharmaceutical manufacturing capabilities.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Agility in Manufacturing
Preparedness Act of 2023''.
SEC. 2. REVIEW OF DOMESTIC BIOPHARMACEUTICAL MANUFACTURING
CAPABILITIES.
(a) In General.--The Secretary of Health and Human Services
(referred to in this section as the ``Secretary''), in cooperation with
the Director of the Biomedical Advanced Research and Development
Authority, shall seek to enter into an agreement with the National
Institute for Innovation in Manufacturing Biopharmaceuticals to perform
the services described in subsection (b).
(b) Review and Recommendations.--Under an agreement described in
subsection (a) between the Secretary, the Director of the Biomedical
Advanced Research and Development Authority, and the National Institute
for Innovation in Manufacturing Biopharmaceuticals, the National
Institute for Innovation in Manufacturing Biopharmaceuticals shall--
(1) review current domestic biopharmaceutical manufacturing
capacity at the Department of Health and Human Services and
such department's adaptability to various threats;
(2) draft recommendations for developing, demonstrating,
deploying, and advancing new domestic biopharmaceutical
manufacturing technologies that address gaps identified under
paragraph (1) and align Federal technologies with technologies
available to the private sector, including through the new
BioMAP initiative of the Biomedical Advanced Research and
Development Authority; and
(3) identify other opportunities and priorities to improve
the United States public health and medical preparedness and
response capabilities and domestic biopharmaceutical
manufacturing capabilities.
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